Canonical Allele Identifier: CA1694876998

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290826_24290828delinsGCA , CM000669.2:g.24290826_24290828delinsGCA	GRCh38
NC_000007.13:g.24330445_24330447delinsGCA , CM000669.1:g.24330445_24330447delinsGCA	GRCh37
NC_000007.12:g.24296970_24296972delinsGCA	NCBI36
NG_016148.1:g.11639_11641delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-837_270-835delinsGCA MANE Select	ENSP00000242152.2:n.270-837_270-835delinsGCA
ENST00000242152.6:c.270-837_270-835delinsGCA	ENSP00000242152.2:n.270-837_270-835delinsGCA
ENST00000405982.1:c.270-837_270-835delinsGCA	ENSP00000385282.1:n.270-837_270-835delinsGCA
ENST00000407573.5:c.270-837_270-835delinsGCA	ENSP00000384364.1:n.270-837_270-835delinsGCA
NM_000905.3:c.270-837_270-835delinsGCA	NP_000896.1:n.270-837_270-835delinsGCA
XM_017012910.1:c.41+28529_41+28531delinsTGC	XP_016868399.1:n.41+28529_41+28531delinsTGC
XM_017012911.1:c.41+28529_41+28531delinsTGC	XP_016868400.1:n.41+28529_41+28531delinsTGC
XR_001745121.1:n.473+28529_473+28531delinsTGC
XR_001745122.1:n.345-93799_345-93797delinsTGC
XR_001745123.1:n.473+28529_473+28531delinsTGC
XR_001745124.1:n.473+28529_473+28531delinsTGC
XR_001745125.1:n.473+28529_473+28531delinsTGC
XR_001745126.1:n.473+28529_473+28531delinsTGC
XR_001745127.1:n.345-35129_345-35127delinsTGC
XR_001745129.1:n.473+28529_473+28531delinsTGC
XR_001745130.1:n.473+28529_473+28531delinsTGC
XR_001745131.1:n.473+28529_473+28531delinsTGC
XR_001745132.1:n.473+28529_473+28531delinsTGC
NM_000905.4:c.270-837_270-835delinsGCA MANE Select	NP_000896.1:n.270-837_270-835delinsGCA